Main article

Mateusz Kowalczyk
Department of Biomedical Engineering, Lublin University of Technology, Lublin 20-618, Poland
Sofia Almeida-Marques
Department of Electrical and Computer Engineering, Polytechnic Institute of Porto (ISEP), Porto 4249-015, Portugal
Daniel J. Pedersen*
Department of Health Informatics, University of Southern Denmark, Odense 5230, Denmark
dpedersen@sdu.dk

DOI: https://doi.org/10.63646/jbda.2023.010105

Abstract

Continuous cardiac monitoring through photoplethysmography (PPG) on consumer wearables has migrated from a fitness convenience to a consequential clinical signal, particularly for screening atrial fibrillation (AF) at population scale. Yet the operating environment of such devices — motion artefacts, perfusion variability, and ambulatory noise — degrades the very deep-learning classifiers that vendors and payers rely on to convert raw waveforms into business and clinical decisions. This article develops a Trust-by-Design Analytics framework for deploying generative artificial intelligence (GenAI) within consumer health wearables, with a specific focus on the AF-screening pipeline. The framework couples a generative adversarial denoiser, a calibrated probabilistic classifier, and a decision-theoretic uncertainty-quantification (DTUQ) layer into a single, cost-sensitive deployment unit. Using a controlled numerical study calibrated to published wearable AF cohorts, we show that DTUQ-gated decisions recover area-under-curve performance from 0.69 under realistic noise to 0.85 after generative reconstruction, while reducing expected misclassification cost by approximately 41% relative to a fixed-threshold baseline at a clinically realistic false-negative-to-false-positive cost ratio of 5:1. We articulate three managerial implications. First, calibration error — not raw accuracy — is the binding constraint on safe scaling of consumer wearables into reimbursable digital-health pathways. Second, the marginal value of a generative denoiser is monotone in the underlying cost asymmetry, which means investment cases for GenAI in this domain must be built on cost-sensitive, not accuracy-sensitive, evaluation. Third, an explicit abstain-and-refer option closes the gap between regulatory expectations for explainable medical AI and the operational reality of always-on consumer sensing. The framework is intended as a deployment template for analytics teams working at the boundary of regulated clinical decision support and at-scale consumer engagement.

Article details

How to Cite

Kowalczyk, M., Almeida-Marques, S. ., & Pedersen, D. J. . (2023). Trust-by-Design Analytics for Consumer Health Wearables: A Cost-Sensitive Framework for Deploying Generative AI in Continuous Cardiac Monitoring. Journal of Business and Data Analytics, 1(1), 69-90. https://doi.org/10.63646/jbda.2023.010105